Literature DB >> 19109024

Synthesis of novel 1,4-benzoxazin-3-one derivatives as inhibitors against tyrosine kinases.

Takahiro Honda1, Takahiro Terao, Hiroyuki Aono, Masakazu Ban.   

Abstract

We designed and synthesized a novel 1,4-benzoxazin-3-one derivative 4 which would have inhibitory activities against tyrosine kinases. They could be synthesized easily from various carboxylic acids 10 and commercially available amines using TFP resin without purification. In this article, we will report the design and synthesis of a novel 1,4-benzoxazin-3-one chemical library 4 and the inhibitory activities against KDR and ABL which are closely related to chronic diseases such as cancer.

Entities:  

Mesh:

Substances:

Year:  2008        PMID: 19109024     DOI: 10.1016/j.bmc.2008.11.060

Source DB:  PubMed          Journal:  Bioorg Med Chem        ISSN: 0968-0896            Impact factor:   3.641


  3 in total

Review 1.  Comprehensive survey of chemical libraries for drug discovery and chemical biology: 2009.

Authors:  Roland E Dolle; Bertrand Le Bourdonnec; Karin Worm; Guillermo A Morales; Craig J Thomas; Wei Zhang
Journal:  J Comb Chem       Date:  2010-10-05

2.  Inhibitors of adenosine consuming parasites through polymer-assisted N-acylation of N6-substituted 5'-amino-5'-deoxyadenosines.

Authors:  Vida Zohrabi-Kalantari; Philipp Heidler; Marcel Kaiser; Reto Brun; Christoph Kamper; Andreas Link
Journal:  Mol Divers       Date:  2009-06-26       Impact factor: 2.943

3.  Synthesis of 2,3-dihydrobenzo[b][1,4]dioxine-5-carboxamide and 3-oxo-3,4-dihydrobenzo[b][1,4]oxazine-8-carboxamide derivatives as PARP1 inhibitors.

Authors:  Xuwei Shao; Steven Pak; Uday Kiran Velagapudi; Shruthi Gobbooru; Sai Shilpa Kommaraju; Woon-Kai Low; Gopal Subramaniam; Sanjai Kumar Pathak; Tanaji T Talele
Journal:  Bioorg Chem       Date:  2020-07-08       Impact factor: 5.307

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.